Canine Dermal Fibroblasts-Adult

Cat.No.: CSC-C4805L

Species: Dog

Source: Dermis; Skin

Cell Type: Fibroblast

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Cat.No.
CSC-C4805L
Description
Canine Dermal Fibroblasts are isolated from skin tissue of beagle dog.
Species
Dog
Source
Dermis; Skin
Cell Type
Fibroblast
Disease
Normal
Quality Control
Canine Dermal Fibroblasts-Adult are negative for bacteria, yeast, fungi, and mycoplasma.
Storage and Shipping
Creative Bioarray ships frozen cells on dry ice. On receipt, immediately transfer frozen cells to liquid nitrogen (-180 °C) until ready for experimental use.
Never can cryopreserved cells be kept at -20 °C.
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Canine Dermal Fibroblasts (CDFs) are a fibroblastic cell line derived from the dermis of healthy adult dogs (Canis lupus familiaris). As the most abundant stromal cell type in the skin, fibroblasts are major contributors to the synthesis of the ECM and influence the architecture and repair of tissues. As expected of fibroblasts, canine dermal fibroblasts have the spindle-shaped adherent morphology of fibroblasts, and will form aligned bundles of cells, or whorls, upon culture surfaces. Similar to fibroblasts from different species, canine dermal fibroblasts proliferate effectively in DMEM or DMEM/F12 with FBS and demonstrate a doubling time between 24-48 hours but their growth rates show variation depending on the donor source and passage level.

Canine dermal fibroblasts produce various ECM components such as collagens I and III, fibronectin, elastin, and glycosaminoglycans while also responding to multiple cytokines and growth factors. Furthermore, canine dermal fibroblasts can be readily induced to differentiate to α-SMA-positive myofibroblasts in response to TGF-β. As such, they are an ideal cell system to study fibrosis, scarring and contractile wound-healing in vitro. Additionally, canine dermal fibroblasts will produce inflammatory cytokines, chemokines, and other mediators such as IL-6, IL-8, and MIP-1α upon stimulation. This allows CDFs to be used in a variety of dermatologic immunology and infection studies. As CDFs have been isolated directly from canine skin tissue and have not been transformed, they maintain many of the physiologically relevant properties of skin tissue. For this reason, CDFs have been used in many applications including veterinary dermatology, wound healing, toxicology and testing of biomaterials, and mechanistic studies of cellular senescence and cellular stress responses.

Effects of Botanical Oleander Extract, Oleandrin and Oclacitinib on Canine Dermal Fibroblast Cytokine Secretion

Canine atopic dermatitis involves cytokine-driven dermal inflammation. Here, Fossum et al. tested oleander extract (OE), oleandrin, and oclacitinib on primary canine dermal fibroblasts and DH82 macrophages under inflamed conditions.

Cytokine levels in supernatants from canine dermal fibroblasts were measured using a canine 11-plex detection kit. Detectable cytokines included IL-6, IL-8, MCP-1 (CCL2), VEGF-A, and SCF. As shown (Fig. 1), all three test products reduced IL-8, MCP-1, and SCF levels. For IL-8, reductions were similar across products. For MCP-1, OE caused the most significant reduction, while for SCF, oleandrin had the greatest effect and OE the mildest. Under LPS-induced inflammation, all products reduced IL-8 secretion, with OE and oleandrin showing robust effects and oclacitinib a mild effect (Fig. 1). VEGF-A levels were significantly reduced by OE and oleandrin, with oleandrin showing statistical significance for both cytokines and OE for MCP-1. Oclacitinib did not affect MCP-1 levels, while OE and oleandrin significantly reduced its secretion (Fig. 2). OE and oleandrin showed anti-inflammatory effects on IL-8 and MCP-1 at a low dose of 0.03 μg/mL, whereas oclacitinib at 0.01 μM was not effective in reducing these cytokines.

Cytokine secretion by canine dermal fibroblasts: heat map showing the levels of significance for changes to cytokine levels in cell cultures treated with oleandrin extract (OE), oleandrin, and oclacitinib.

Fig. 1. Cytokine secretion by canine dermal fibroblasts: heat map showing the levels of significance for changes to cytokine levels in cell cultures treated with oleandrin extract (OE), oleandrin, and oclacitinib (Fossum W. T, Jense S. G, et al., 2024).

Cytokine secretion by canine dermal fibroblasts: changes to cytokine production by canine DH82 macrophage cells under inflamed culture conditions.

Fig. 2. Cytokine secretion by canine dermal fibroblasts: changes to cytokine production by canine DH82 macrophage cells under inflamed culture conditions (Fossum W. T, Jense S. G, et al., 2024).

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